Device Classification Name |
goniometer, ac-powered
|
510(k) Number |
K961212 |
Device Name |
SPINAL TOUCH |
Applicant |
FASSTECH |
155 MIDDLESEX TURNPIKE |
BURLINGTON,
MA
01803
|
|
Applicant Contact |
LEE R BRODY |
Correspondent |
FASSTECH |
155 MIDDLESEX TURNPIKE |
BURLINGTON,
MA
01803
|
|
Correspondent Contact |
LEE R BRODY |
Regulation Number | 888.1500
|
Classification Product Code |
|
Date Received | 03/28/1996 |
Decision Date | 06/12/1996 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Orthopedic
|
510k Review Panel |
Neurology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|